Smad-Independent BMP Signaling in Somatic Cells Limits the Size of the Germline Stem Cell Pool

• Main Authors: Chen-Yuan Tseng, Yu-Han Su, Shun-Min Yang, Kun-Yang Lin, Chun-Ming Lai, Elham Rastegari, Oyundari Amartuvshin, Yueh Cho, Yu Cai, Hwei-Jan Hsu
• Format: Article
• Language: English
• Published: Elsevier 2018-09-01
• Series: Stem Cell Reports
• Online Access: http://www.sciencedirect.com/science/article/pii/S2213671118303138

Summary: In developing organisms, proper tuning of the number of stem cells within a niche is critical for the maintenance of adult tissues; however, the involved mechanisms remain largely unclear. Here, we demonstrate that Thickveins (Tkv), a type I bone morphogenetic protein (BMP) receptor, acts in the Drosophila developing ovarian soma through a Smad-independent pathway to shape the distribution of BMP signal within the niche, impacting germline stem cell (GSC) recruitment and maintenance. Somatic Tkv promotes Egfr signaling to silence transcription of Dally, which localizes BMP signals on the cell surface. In parallel, Tkv promotes Hh signaling, which promotes escort cell cellular protrusions and upregulates expression of the Drosophila BMP homolog, Dpp, forming a positive feedback loop that enhances Tkv signaling and strengthens the niche boundary. Our results reveal a role for non-canonical BMP signaling in the soma during GSC establishment and generally illustrate how complex, cell-specific BMP signaling mediates niche-stem cell interactions. : In this article, Hsu and her colleagues show that Tkv, a type I BMP receptor, functions in the developing ovarian soma to control the size of germline stem cell (GSC) pool via a Smad-independent pathway. BMP-Tkv signaling in the soma limits BMP signals within the GSC niche via Egfr and Hh signaling to ensure that germ cells outside of the niche undergo proper differentiation. Keywords: PGC, GSC, niche, Egfr, Hh, BMP, soma-germline interaction, escort cells